Dataset

The dataset mentioned in [1] and [3] is available for download. If you use this dataset in your work, please cite [3].

References

If you use DINC in your work, please cite [1]

The underlying methods of DINC are presented in greater details in [1]. The functionalities of the webserver are described in [2]

To learn more about the challenges of protein flexibility in molecular docking, please read [4].

1. D. Devaurs, D.A. Antunes, S. Hall-Swan, N. Mitchell, M. Moll, G. Lizée, and L. E. Kavraki, “Using parallelized incremental meta-docking can solve the conformational sampling issue when docking large ligands to proteins," BMC Molecular and Cell Biology, vol. 20, no. 1, p. 42, 2019.
   
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2. D. A. Antunes, M. Moll, D. Devaurs, K. R. Jackson, G. Lizée, and L. E. Kavraki, “DINC 2.0: a new protein-peptide docking webserver using an incremental approach,” Cancer Research, vol. 77, no. 21, pp. e55–57, 2017.
   
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3. A. Dhanik, J. McMurray, and L. E. Kavraki, “DINC: A new AutoDock-based protocol for docking large ligands,” BMC Structural Biology, vol. 13, no. Suppl 1, p. S11, 2013.
   
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4. D. A. Antunes, D. Devaurs, and L. E. Kavraki, “Understanding the challenges of protein flexibility in drug design,” Expert Opinion on Drug Discovery, vol. 10, no. 12, pp. 1301–1313, 2015.
   
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